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rs727505368

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505368(G;T)
Make rs727505368(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position37253847
is asnp
is mentioned by
dbSNPrs727505368
ebirs727505368
HLIrs727505368
Exacrs727505368
Varsomers727505368
Maprs727505368
PheGenIrs727505368
hapmaprs727505368
1000 genomesrs727505368
hgdprs727505368
ensemblrs727505368
gopubmedrs727505368
geneviewrs727505368
scholarrs727505368
googlers727505368
pharmgkbrs727505368
gwascentralrs727505368
openSNPrs727505368
23andMers727505368
23andMe allrs727505368
SNP Nexus

SNPshotrs727505368
SNPdbers727505368
MSV3drs727505368
GWAS Ctlgrs727505368
Max Magnitude0
ClinVar
Risk rs727505368(T;T)
Alt rs727505368(T;T)
Reference rs727505368(G;G)
Significance Probable-Pathogenic
Disease Delayed puberty
Variation info
Gene
CLNDBN Delayed puberty
Reversed 0
HGVS NC_000012.12:g.37253847G>T
CLNSRC
CLNACC RCV000156949.1,